(4S)-3-[(2S,3R)-2-(cyclopenten-1-yl)-3-hydroxybutanoyl]-4-propan-2-yl-1,3-oxazolidin-2-one | 192329-13-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑烷类
• 英文名称: (4S)-3-[(2S,3R)-2-(cyclopenten-1-yl)-3-hydroxybutanoyl]-4-propan-2-yl-1,3-oxazolidin-2-one
• CAS: 192329-13-8
• 化学式: C₁₅H₂₃NO₄
• 分子量: 281.352
• InChiKey: ODHJQZHEWVWOTM-RAIGVLPGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  20
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  66.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (4S)-3-[(2S,3R)-2-(cyclopenten-1-yl)-3-hydroxybutanoyl]-4-propan-2-yl-1,3-oxazolidin-2-one 在 碘 、 碳酸氢钠 作用下， 以 乙腈 为溶剂， 反应 12.0h， 以83%的产率得到(4S)-3-[(2R,3S,3aS,6aR)-3a-iodo-2-methyl-2,3,4,5,6,6a-hexahydrocyclopenta[b]furan-3-carbonyl]-4-propan-2-yl-1,3-oxazolidin-2-one
  参考文献：
  名称：

  Enantioselective Construction of Cyclic Ethers by An Aldol-Cyclization Sequence

  摘要：

  We have modified the substrate used in deconjugative aldol-cyclizations by incorporating the Evans chiral auxiliary. The deconjugative aldol step, using boron enolates, gave the expected products with complete syn-aldol stereochemistry. These compounds could then undergo an iodine-mediated cyclization to form optically active products. Oxetanes and fused ring tetrahydrofurans were easily assembled with a variety of substitution patterns and with excellent enantiocontrol. The deconjugation of acyclic chiral enimides resulted in the loss of control of olefin geometry. However, these compounds did appear to cyclize with excellent enantiocontrol.

  DOI：

  10.1021/jo961904z
• 作为产物：
  描述：

  (S)-4-异丙基-2-唑烷酮 在 正丁基锂 、 三氟甲磺酸二丁硼 、 三乙胺 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 3.75h， 生成 (4S)-3-[(2S,3R)-2-(cyclopenten-1-yl)-3-hydroxybutanoyl]-4-propan-2-yl-1,3-oxazolidin-2-one
  参考文献：
  名称：

  Enantioselective Construction of Cyclic Ethers by An Aldol-Cyclization Sequence

  摘要：

  We have modified the substrate used in deconjugative aldol-cyclizations by incorporating the Evans chiral auxiliary. The deconjugative aldol step, using boron enolates, gave the expected products with complete syn-aldol stereochemistry. These compounds could then undergo an iodine-mediated cyclization to form optically active products. Oxetanes and fused ring tetrahydrofurans were easily assembled with a variety of substitution patterns and with excellent enantiocontrol. The deconjugation of acyclic chiral enimides resulted in the loss of control of olefin geometry. However, these compounds did appear to cyclize with excellent enantiocontrol.

  DOI：

  10.1021/jo961904z